2033-87-6 Usage
Uses
Used in Organic Synthesis:
10-Phenoxydecyl bromide is utilized as a key intermediate in the synthesis of various organic compounds, particularly those requiring the introduction of a brominated alkyl chain with a phenoxy group. Its unique structure makes it a valuable building block in the creation of complex organic molecules.
Used in Organic Chemistry Reactions:
As a reagent in organic chemistry, 10-Phenoxydecyl bromide is employed in a range of reactions, including alkylation, where it can transfer an alkyl group to another molecule. This property is particularly useful in the preparation of pharmaceuticals, agrochemicals, and other specialty chemicals that require specific functional groups.
Used in Pharmaceutical Industry:
10-Phenoxydecyl bromide is used as a precursor in the development of pharmaceutical compounds, where its alkylating ability can be harnessed to modify the structure of drug molecules, potentially enhancing their therapeutic effects or improving their pharmacokinetic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 10-Phenoxydecyl bromide serves as a starting material for the synthesis of active ingredients in pesticides and herbicides. Its reactivity allows for the creation of new molecules with targeted pest control capabilities.
Used in Specialty Chemicals:
10-Phenoxydecyl bromide is also used in the production of specialty chemicals, such as dyes, fragrances, and other additives, where its unique structure can impart specific properties to the final product.
Check Digit Verification of cas no
The CAS Registry Mumber 2033-87-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,3 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2033-87:
(6*2)+(5*0)+(4*3)+(3*3)+(2*8)+(1*7)=56
56 % 10 = 6
So 2033-87-6 is a valid CAS Registry Number.
2033-87-6Relevant academic research and scientific papers
Encapsulating propeller-like columnar liquid crystals with an aromatic outer shell: Influence of phenoxy-terminated side chains on the phase behaviour of triphenylbenzenes
Bader, Korinna,W?hrle, Tobias,?ztürk, Esra,Baro, Angelika,Laschat, Sabine
, p. 6409 - 6414 (2018/08/17)
Tailoring of phase transition temperatures of columnar liquid crystals by side chain variation is often associated with an undesired change in the mesophase type and/or geometry. To overcome this problem phenoxy-terminated side chains rather than alkyl si
2,2-Dichloroalkanecarboxylic acids, processes for their production and pharmaceutical agents containing these
-
, (2008/06/13)
Pharmaceutical agents for treating diabetus mellitus which contain a compound of formula I STR1 as the active substance, in which A, B, A' and W have the meanings stated in the claims, new compounds of formula I as well as processes for their production.
ω-Substituted alkyl carboxylic acids as antidiabetic and lipid-lowering agents
Meyer, Kirstin,Voss, Edgar,Neidlein, Richard,Kuehnle, Hans-Frieder,Pill, Johannes
, p. 775 - 787 (2007/10/03)
In screening experiments certain ω-substituted alkyl carboxylic acids were found to produce an increase in insulin-stimulated 14C-acetate incorporation into triglycerides, which may indicate an improvement in the action of insulin. Antidiabetic
The mechanism of the photo-induced homolysis of aryl halides
Davidson, R.Stephen,Goodin, Jonathan W.,Kemp, Graham
, p. 2911 - 2914 (2007/10/02)
Irradiation of the ω-(4-halophenoxy)alkyl bromides (Ia,b n=10) in methanol usually leads to preferential cleavage of the aryl-halogen bond and data is presented supporting the conclusion that this occurs from the first excited single state.
